期刊文献+

负载辅酶Q10的两亲性聚肽-壳聚糖复合纳米粒的制备及性质研究 被引量:1

Preparation and Characterization of Amphiphilic Polypeptide-chitosan Complex Nanoparticles Containing Coenzyme Q10
下载PDF
导出
摘要 以两亲性聚肽-壳聚糖复合体系为壁材,采用自组装及离子凝聚法制备负载辅酶Q10的纳米粒子,探讨了制备纳米粒子的较佳条件,采用高分辨率透射电镜、动态激光散射仪、紫外光谱及Zeta电位分析仪对优化的聚肽-壳聚糖复合体系纳米粒子进行表征,结果表明:聚肽-壳聚糖复合体系纳米粒子是具有壳核结构的球型粒子;纳米粒子粒径大小在80 nm到300 nm之间,粒径分布较均匀,稳定性较好,粒子的载药率为3.46±0.3%,包封率为59.7±2.1%。24 h的累积释放为75%。 Biocompatible amphiphilic polypeptide-chitosan was used to prepare nanoparticles containing coenzyme Q10 by self-assembly and ion gel methods. The optimal preparation conditions of polypeptidechitosan complex nanoparticles were investigated. The properties of nanoparticles containing coenzyme Q10 were studied by transmission electron microscopy, dynamic light scattering, ultraviolet-visible spectroscopy and zeta potential analyzer. The results showed that the morphology of the nanoparticles is spherical with a shell-core structure, the size of the nanoparticles is from 80 nm to 300 nm, and the distribution is homogeneous. The particles have good stability. The drug-loading amount of coenzyme Q10 is 3.46±0.3%, the entrapment efficiency is 59.7±2.1%, and the 24 h accumulative in vitro release is 75%.
出处 《化学世界》 CAS CSCD 北大核心 2009年第9期521-524,517,535,共6页 Chemical World
基金 上海市教育委员会自然基金资助项目(06OZ005)
关键词 两亲性聚肽共聚物 壳聚糖 辅酶Q10 纳米粒子 amphiphilic polypeptide copolymer chitosan coenzyme Q10 nanoparticles
  • 相关文献

参考文献10

  • 1Ikematsu H, Nakamura K, Harashima S, et al. "Safety assessment of coenzyme Q10 (Kaneka Q10) in healthy subjects: A double-blind, randomized, placebo-controlled trial [ J ]. Regulatory Toxicology and Pharmacology, 2006, 44(3) :212-218. 被引量:1
  • 2Blatt T, Wittem K P, Wenck H, et al. CoQ10, a topical energizer for aging skin[J]. Journal of the American Academy of Dermatology, 2004, 50 (3) Supplement 1:76. 被引量:1
  • 3Yan J M, Fujii K, Yao J J, etal. Reduced coenzyme Q10 supplementation decelerates senescence in SAMP1 mice[J]. Experimental Gerontology, 2006, 41(2): 130-140. 被引量:1
  • 4Yokoyama M. Drug targeting with nancrsized carder systems[J]. J Artif Organs, 2005, 8(2) :77-84. 被引量:1
  • 5冯敏,潘仕荣,张静夏,王琴梅,吴伟荣,李瑞明.两性霉素B/聚乙二醇-聚谷氨酸苄酯纳米粒的体外细胞摄取研究[J].中国药科大学学报,2005,36(4):321-325. 被引量:12
  • 6Tang D M, Lin J P, Lin S L, etal. Self-assembly of poly ( benzyl-L-glutamate )-grafi-poly ( ethylene glycol) and its mixtures with poly (benzyl-L- glutamate ) homopolymer[ J]. Macromol Rapid Commun, 2004, 25(13): 1241-1246. 被引量:1
  • 7章苏宁,陈涛,林嘉平,董秀斌,林绍梁.两亲性聚(L-谷氨酸γ-苄基酯)-聚乙二醇接枝共聚物的自组装行为和载药性能研究[J].高分子学报,2005,15(6):929-932. 被引量:6
  • 8Bozkir A, Saka O M. Chitosan nanopartieles for plasmid DNA delivery: effect of ehitosan molecular structure on formulation and release characteristics [J]. Drug Delivery, 2004, 11(2) : 107-112. 被引量:1
  • 9Bravo-Osuna I, Schmitz T, Bernkop-Schntirch A, et al. Elaboration and characterization of thiolated ehitosan-coated acrylic nanoparticles[J]. International Journal of Pharmaceutics, 2006, 316(1-2): 170-175. 被引量:1
  • 10Shi X W, Du Y M, Sun L P, et al. Polyelectrolyte complex beads composed of water-soluble chitosan/ alginate: Characterization and their protein release behavior[J]. J Appl PolymSci, 2006, 100(6):4614- 4622. 被引量:1

二级参考文献26

  • 1冯敏,潘仕荣,吴伟荣.两性霉素B/聚乙二醇-聚谷氨酸苄酯纳米球溶血毒性的研究[J].中国药科大学学报,2004,35(3):263-266. 被引量:6
  • 2Yoo HS, Lee KH, Oh JE, et al. In vitro and in vivo anti-tumor activities of nanoparticles based on doxorubicin-PLGA conjugates[J]. J Controlled Release, 2000,68 ( 3 ): 419 - 431. 被引量:1
  • 3Tobio M, Gref R, Sanchez A, et al. Stealth PLA-PEG nanoparticles as protein cariers for nasal administration [ J]. Pharm Res, 1998, 15(2) :270 - 275. 被引量:1
  • 4Bazile D, Prudhomme C, Bassoullet MT, et al. Stealth Me. PEG-PLA nanoparticles avoid uptake by the mononuclear phagocytes system[J]. J Pharm Sci, 1995,84(4) :493 - 498. 被引量:1
  • 5Kwon GS, kataoka K. Block copolymer micelles as long-circulating drug vehicles[J]. Adv Drug Delivery Rev, 1995,16(2 - 3 ): 295 -309. 被引量:1
  • 6Rudt S, Muller RH. In vitro phagocytosis assay of nano and microparticles by chemiluminescencs. Ⅱ. Effect of surface modification by coating of particles with poloxamer on the phagocytic uptake[J]. J Controlled Release, 1993,25( 1 ) :51 - 59. 被引量:1
  • 7Illum L, Humneyball IM, Davis SS. The effect of hydrophilic coating on the uptake of colloidal particles by the liver and by peritoneal macrophages[ J]. Iht J Pharm, 1986,29(1):53 - 65. 被引量:1
  • 8Illum L, Davis SS. Effect of the nonionic surfactant poloxamer 338 on the fate and deposition of polystyrene microspheres following administration[J]. J Pharm Sci, 1983,72(9): 1 086 - 1 089. 被引量:1
  • 9Esposito E, Bortolotti F, Menegatti E. Amphiphilic association systems for amphotericin B delivery [J]. Int J Pharm,2003,260(2) :249 -260. 被引量:1
  • 10Cho C S, Park I K, Nab J W, Akaike T. Macromolecular Research,2003,11:2 - 8. 被引量:1

共引文献16

同被引文献5

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部